Súlyos hereditaer V. factor-hiányos beteg esetének ismertetese.

Translated title of the contribution: Severe congenital factor V deficiency: case report

Marosi Anikó, Apjok Eniko, Magyarosy Edina, T. Szabó, E. Ajzner

Research output: Contribution to journalArticle

Abstract

Introduction: Congential deficiency of factor V is a rare condition, transmitted in autosomal recessive way. Heterozygote patients generally have no symptoms, homozygotes present with spontaneous and postoperative bleedings. About one-half of patients are diagnosed in adulthood. Methods: The presented case is a double heterozygote, which was confirmed using moleculare biological methods. The authors found many carriers in his family. Conclusions: This rare and sometimes severe disorder needs regular haematological controls. Carriers must have more attention during surgical procedures and labour, and the family doctor should be informed about there condition.

Original languageHungarian
Pages (from-to)87-89
Number of pages3
JournalOrvosi Hetilap
Volume143
Issue number2
Publication statusPublished - Jan 13 2002

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Factor V Deficiency
Heterozygote
Homozygote
Hemorrhage

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Súlyos hereditaer V. factor-hiányos beteg esetének ismertetese. / Anikó, Marosi; Eniko, Apjok; Edina, Magyarosy; Szabó, T.; Ajzner, E.

In: Orvosi Hetilap, Vol. 143, No. 2, 13.01.2002, p. 87-89.

Research output: Contribution to journalArticle

Anikó, M, Eniko, A, Edina, M, Szabó, T & Ajzner, E 2002, 'Súlyos hereditaer V. factor-hiányos beteg esetének ismertetese.', Orvosi Hetilap, vol. 143, no. 2, pp. 87-89.
Anikó, Marosi ; Eniko, Apjok ; Edina, Magyarosy ; Szabó, T. ; Ajzner, E. / Súlyos hereditaer V. factor-hiányos beteg esetének ismertetese. In: Orvosi Hetilap. 2002 ; Vol. 143, No. 2. pp. 87-89.
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